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Cas:16724-63-3
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
Cas:16724-63-3
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou
1.Our services:A.Supply sampleB.The packing also can be according the customers` requirmentC.Any inquiries will be replied within 24 hoursD.we provide Commerical Invoice, Packing List, Bill of loading, COA , Health certificate and Origin certificate.
Cas:16724-63-3
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Cas:16724-63-3
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inquiryWe product this chemical more than 10 years . We are very experience to export it to many countries, Our superior & stable quality , competitive price gain warm reception from our customers. Application:Chemical intermediate
We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:off-white powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use as prima
Supply top quality products with a reasonable price Application:api
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Price, service, company and transport advantage: 1. Best service, place of origin China, high quality, and reasonable price. 2. It's customers' right to choose the package (EMS, DHL, FEDEX, UPS). 3. It's customers' right
United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
Cas:16724-63-3
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Type:Lab/Research institutions
inquiry1-Hexadecanamine,N-hexadecyl- Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/She
Manufacturer,strong R&D,professional team Storage:Store in a cool, dry place. Store in a tightly closed container. Package:according to your requirement Application:ZhiShang Chemical is owned by ZhiShang Group, is a professional new-type chemicals en
hexadecylamine
dihexadecylamine
Conditions | Yield |
---|---|
With Co2Rh2/C In toluene at 180℃; under 760.051 Torr; for 18h; Autoclave; Inert atmosphere; | 97% |
In aluminum nickel; water; benzene | 73% |
With nickel at 200℃; |
Conditions | Yield |
---|---|
With platinum-titanium/titanium oxide catalyst In toluene at 120℃; for 48h; Temperature; Solvent; Reagent/catalyst; Sealed tube; | 95% |
N,N-Dihexadecyl-2-(tetrahydro-pyran-2-yloxymethyl)-benzamide
dihexadecylamine
Conditions | Yield |
---|---|
With water; acetic acid In tetrahydrofuran at 60℃; for 4h; | 76% |
Conditions | Yield |
---|---|
Stage #1: hexadecylamine; n-hexadecanoyl chloride With dmap; triethylamine In toluene at 20℃; for 48h; Stage #2: With lithium aluminium tetrahydride In tetrahydrofuran for 18h; Heating; | 65% |
Stage #1: hexadecylamine; n-hexadecanoyl chloride Stage #2: With lithium aluminium tetrahydride Further stages.; | |
Multi-step reaction with 2 steps 1: triethylamine / dichloromethane / 20 °C 2: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C View Scheme |
Conditions | Yield |
---|---|
With sodium carbonate In ethanol for 116h; Reflux; | 59% |
With potassium carbonate In ethanol for 120h; Reflux; | 50.2% |
With sodium carbonate In ethanol for 116h; Heating; | 27% |
With sodium carbonate |
hexadecylamine
1-iodohexadecane
A
dihexadecylamine
B
trihexadecylamine
Conditions | Yield |
---|---|
at 180℃; |
Conditions | Yield |
---|---|
With ethanol; ammonia at 170℃; |
palmitanilide
dihexadecylamine
Conditions | Yield |
---|---|
With 1,4-dioxane; Ba containing copper chromite at 270 - 290℃; under 154457 Torr; Hydrogenation; |
sodium cyanamide
hexadecanyl bromide
dihexadecylamine
Conditions | Yield |
---|---|
With ethanol Kochen des gebildeten Dihexadecyl-cyanamids mit verd. H2SO4; |
Palmitamide
dihexadecylamine
Conditions | Yield |
---|---|
With 1,4-dioxane; Ba containing copper chromite at 270 - 290℃; under 154457 Torr; Hydrogenation; | |
With zinc oxide-chromium oxide at 315 - 330℃; under 147102 - 176522 Torr; Hydrogenation; | |
Multi-step reaction with 3 steps 1: lithium aluminium tetrahydride / tetrahydrofuran / 1 h 2: triethylamine / dichloromethane / 20 °C 3: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C View Scheme | |
With nickel at 225 - 245℃; under 125036 - 147102 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
at 270 - 280℃; under 73550.8 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
at 200℃; |
ethanol
1-Chlorohexadecan
ammonia
A
hexadecylamine
B
dihexadecylamine
Conditions | Yield |
---|---|
at 170℃; |
dihexadecylamine
Conditions | Yield |
---|---|
With sodium tetrahydroborate In methanol; dichloromethane at 20℃; for 4h; | |
With sodium tetrahydroborate In methanol; dichloromethane at 0 - 20℃; for 4h; |
Dihexadecyl-cyanamide
dihexadecylamine
Conditions | Yield |
---|---|
With sulfuric acid for 8h; Heating; | 35.8 g |
hexadecanyl bromide
dihexadecylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: NaOH; Aliquat 336 / H2O; toluene / 8 h / 50 °C 2: 35.8 g / aq. H2SO4 / 8 h / Heating View Scheme |
n-hexadecylaldehyde
dihexadecylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: MgSO4 / CH2Cl2 / 0 - 20 °C 2: NaBH4 / CH2Cl2; methanol / 4 h / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: MgSO4 / CH2Cl2 / 3 h / 0 - 20 °C 2: NaBH4 / CH2Cl2; methanol / 4 h / 0 - 20 °C View Scheme |
methanesulfonic acid hexadecyl ester
dihexadecylamine
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: t-BuOK / dimethylformamide / 1 h / Ambient temperature 2: NaBH4 / propan-2-ol; toluene; H2O / 4 h / 0 °C 3: p-TsOH / CH2Cl2 / 2 h / Ambient temperature 4: 73 percent / dimethylformamide / 6 h / 40 °C 5: 76 percent / AcOH, H2O / tetrahydrofuran / 4 h / 60 °C View Scheme |
N-hexadecyl-phthalimide
dihexadecylamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: NaBH4 / propan-2-ol; toluene; H2O / 4 h / 0 °C 2: p-TsOH / CH2Cl2 / 2 h / Ambient temperature 3: 73 percent / dimethylformamide / 6 h / 40 °C 4: 76 percent / AcOH, H2O / tetrahydrofuran / 4 h / 60 °C View Scheme |
N-Hexadecyl-2-hydroxymethyl-benzamide
dihexadecylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: p-TsOH / CH2Cl2 / 2 h / Ambient temperature 2: 73 percent / dimethylformamide / 6 h / 40 °C 3: 76 percent / AcOH, H2O / tetrahydrofuran / 4 h / 60 °C View Scheme |
N-Hexadecyl-2-(tetrahydro-pyran-2-yloxymethyl)-benzamide
dihexadecylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 73 percent / dimethylformamide / 6 h / 40 °C 2: 76 percent / AcOH, H2O / tetrahydrofuran / 4 h / 60 °C View Scheme |
n-hexadecanoyl chloride
dihexadecylamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: ammonia / dichloromethane 2: lithium aluminium tetrahydride / tetrahydrofuran / 1 h 3: triethylamine / dichloromethane / 20 °C 4: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: triethylamine / tetrahydrofuran; N,N-dimethyl-formamide / 21 h / 0 - 20 °C 2: lithium aluminium tetrahydride / tetrahydrofuran / 12 h / 55 °C View Scheme |
N-(hexadecanoyl)hexadecylamide
dihexadecylamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 20℃; | |
With lithium aluminium tetrahydride In tetrahydrofuran at 55℃; for 12h; |
1-hexadecylcarboxylic acid
dihexadecylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: oxalyl dichloride / benzene / 3 h 2: triethylamine / dichloromethane / 20 °C 3: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C View Scheme | |
Multi-step reaction with 5 steps 1: oxalyl dichloride / benzene / 3 h 2: ammonia / dichloromethane 3: lithium aluminium tetrahydride / tetrahydrofuran / 1 h 4: triethylamine / dichloromethane / 20 °C 5: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C View Scheme |
Conditions | Yield |
---|---|
With ammonium hydroxide; hydrogen at 220℃; under 41254.1 Torr; for 36h; Autoclave; | A 54 %Chromat. B 19 %Chromat. |
dihexadecylamine
Boc-His(Tos)-OH
Conditions | Yield |
---|---|
With diethyl cyanophosphonate; triethylamine In dichloromethane at 0 - 25℃; for 1.5h; | 99% |
4-(Dichloromethyl)phenoxy acetyl chloride
dihexadecylamine
N,N-dihexadecyl-4-(dichloromethyl)phenoxy acetamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane | 92% |
succinic acid anhydride
dihexadecylamine
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 24h; | 90.6% |
In tetrahydrofuran at 20℃; for 18h; | 86.1% |
In tetrahydrofuran at 20℃; for 24h; | 78.8% |
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In dichloromethane 1.) 0 deg C, 2 h, 2.) r.t., 15 h; | 90% |
dihexadecylamine
epichlorohydrin
N,N-dihexadecyl(oxyranylmethyl)amine
Conditions | Yield |
---|---|
at 30 - 70℃; for 16h; | 84% |
1,4-dioxane-2,6-dione
dihexadecylamine
di-n-hexadecylcarbamoylmethoxyacetic acid
Conditions | Yield |
---|---|
In tetrahydrofuran for 48h; Heating; | 80% |
dihexadecylamine
trihexadecylamine
Conditions | Yield |
---|---|
With Co2Rh2/C In toluene at 180℃; under 760.051 Torr; for 18h; Autoclave; Inert atmosphere; | 74% |
Conditions | Yield |
---|---|
Stage #1: succinic acid anhydride; dihexadecylamine In toluene at 20℃; for 48h; Stage #2: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In ethanol; toluene for 3.5h; Stage #3: 3-aminopropyltriethoxysilane In ethanol; toluene at 20℃; for 48h; Solvent; Reagent/catalyst; Molecular sieve; | 68.5% |
Condensation; |
dihexadecylamine
3-bromo-isocyanatopropane
3-(3-bromopropyl)-1,1-dihexadecylurea
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 3h; | 67% |
dihexadecylamine
Boc-Glu(OBzl)-OH
N,N-dihexadecyl-Nα-tert-butoxycarbonyl-O-benzyl-L-glutamic acid α-amide
Conditions | Yield |
---|---|
Stage #1: Boc-Glu(OBzl)-OH With dicyclohexyl-carbodiimide In dichloromethane at 0℃; for 0.5h; Stage #2: dihexadecylamine In dichloromethane at 20℃; | 66% |
dihexadecylamine
3-(bromomethyl)benzonitrile
α-[N,N-di(n-hexadecyl)amino]-m-toluonitrile
Conditions | Yield |
---|---|
With potassium carbonate In hexane; ISOPROPYLAMIDE | 62% |
With potassium carbonate In N,N-dimethyl acetamide; acetone |
BOC-glycine
dihexadecylamine
N,N-dihexadecyl-Nα-(tert-butoxycarbonyl)glycinamide
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 16h; | 61.8% |
succinic acid anhydride
dihexadecylamine
2-aminoethyl O-2',3',4',6'-tetraacetyl-β-D-glucopyranoside
Conditions | Yield |
---|---|
Multistep reaction.; | 60% |
dihexadecylamine
Boc-(S)-Lys(2-Cl-Z)-OH
N,N-dihexadecyl-Nα-tert-butoxycarbonyl-Nε-2-chlorobenzyloxycarbonyl-L-lysine amide
Conditions | Yield |
---|---|
Stage #1: Boc-(S)-Lys(2-Cl-Z)-OH With dicyclohexyl-carbodiimide In dichloromethane at 0℃; for 0.5h; Stage #2: dihexadecylamine In dichloromethane at 20℃; | 59% |
dihexadecylamine
11-(t-butoxycarbonylamino)-3,6,9-trioxaundecanoic acid-dicyclohexylammonium salt
Conditions | Yield |
---|---|
Stage #1: 11-(t-butoxycarbonylamino)-3,6,9-trioxaundecanoic acid-dicyclohexylammonium salt With 1,1'-carbonyldiimidazole In tetrahydrofuran at 0 - 25℃; for 1h; Stage #2: dihexadecylamine at 20 - 40℃; for 8h; | 59% |
dihexadecylamine
3-tert-butyldimethylsilyloxy-17α-[3-aldehydopropane]-17β-estradiol
3-tert-butyldimethylsilyloxy-17α-[3-N,N-dihexadecyl(amino)propane]-17β-estradiol
Conditions | Yield |
---|---|
Stage #1: dihexadecylamine; 3-tert-butyldimethylsilyloxy-17α-[3-aldehydopropane]-17β-estradiol In dichloromethane at 20℃; for 0.5h; Stage #2: With sodium cyanoborohydride In dichloromethane for 24h; | 57.3% |
dihexadecylamine
dicyclohexylammonium 1-(tert-butyloxycarbonylamino)-3,6-dioxa-octanoate
Conditions | Yield |
---|---|
Stage #1: dicyclohexylammonium 1-(tert-butyloxycarbonylamino)-3,6-dioxa-octanoate With 1,1'-carbonyldiimidazole In tetrahydrofuran at 0 - 25℃; for 1h; Stage #2: dihexadecylamine In tetrahydrofuran at 20 - 50℃; for 19h; | 55% |
dihexadecylamine
Boc-His(Bzl)-OH
N,N-dihexadecyl-Nα-(t-butoxycarbonyl)-Nim-benzyl-L-histidinamide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In dichloromethane 1) 3 h; 0 deg C; 2) 15 h; room temp.; | 54% |
dihexadecylamine
2-(tert-butyldimethylsilyloxy)ethyl bromide
O-tert-butyldimethylsilyl N-2-hydroxyethyl-N,N-di-n-hexadecylamine
Conditions | Yield |
---|---|
With potassium carbonate In ethyl acetate for 40h; Heating; | 46% |
dihexadecylamine
N(α)-t-butoxycarbonyl-N(ϖ)-benzyloxymethyl-L-histidine
N,N-dihexadecyl-Nα-tert-butoxycarbonyl-Nim-benzyloxymethyl-L-histidine amide
Conditions | Yield |
---|---|
With diethyl cyanophosphonate; triethylamine In dichloromethane at 20℃; for 2h; | 46% |
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 45h; | 31% |
dihexadecylamine
2,2:4,5-di-O-isopropylidene-D-arabinose
Dihexadecyl-((4S,5R,4'R)-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl]-5-ylmethyl)-amine
Conditions | Yield |
---|---|
Stage #1: dihexadecylamine; 2,2:4,5-di-O-isopropylidene-D-arabinose In dichloromethane for 0.5h; Stage #2: With sodium cyanoborohydride In dichloromethane at 20℃; for 30h; Further stages.; | 40% |
dihexadecylamine
1-aldehydo-2,3:5,6-diisopropylidene-4-(tert-butyl-dimethylsilyloxy)-D-galactose
1-deoxy-1-[di-n-hexadecyl(amino)]-2,3:5,6-diisopropylidene-4-(tert-butyl-dimethylsilyloxy)-D-galactose
Conditions | Yield |
---|---|
Stage #1: dihexadecylamine; 1-aldehydo-2,3:5,6-diisopropylidene-4-(tert-butyl-dimethylsilyloxy)-D-galactose In dichloromethane at 20℃; for 0.5h; Stage #2: With sodium cyanoborohydride In dichloromethane for 24h; | 24% |
formaldehyd
formic acid
dihexadecylamine
N-hexadecyl-N-methylhexadecan-1-amine
Conditions | Yield |
---|---|
With ethanol anfangs auf 40-60grad,zuletzt auf Siedetemperatur; |
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